International safety notice
Technical name: Vascular Endoprosthesis
Brazil / Anvisa · BRA · Mar 2, 2017
Key facts
| Title | Technical name: Vascular Endoprosthesis |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Endurant / Endurant II Endoprotese system Technical name: Vascular Endoprotese ANVISA registration number: 10339190330/ 10339190508 Risk class: IV Affected model: ENBF2313C120EE; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO MEDTRONIC COMERCIAL LTDA ENDEREÇO AV JORNALISTA ROBERTO MARINHO 85 10º ANDAR CEP 04675010 SP CONTATO 11 21829200 FABRICANTE MEDTRONIC IRELAND PARKMORE BUSINESS PARK WEST GALWAY IRLANDA MEDTRONIC MEXICO AVENIDA PASEO DEL CUCAPAH 10510 PARQUE INDUSTRIAL EL LAGO TIJUANA BC 22570 M MEXICO MEDTRONIC INC 710 MEDTRONIC PARKWAY NE MINNIAPOLIS MN 55432 |
| Models | ETBF2313C166EE, ETBF2316C166E, ETBF2516C145EE, ETBF2516C124EE, 10339190330, ENBF2316C145EE, ETBF2313C124E, ETBF2513C166EE, ETBF2516C145E, ENBF2513C170EE, ENBF2516C145EE, ETBF2313C124EE and 16 more |
| Date | Mar 2, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1